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嚢胞性線維症患者に対する運動と気道確保技術の比較

2 years 11 months ago
嚢胞性線維症患者に対する運動と気道確保技術の比較 レビューの論点 嚢胞性線維症(CF)患者にとって、運動は他の気道確保法に取って代わることができるか? 背景 嚢胞性線維症(CF)は、多くの身体のシステムに悪影響を与えるが、主に肺に悪影響を与える。肺に粘着性のある濃い粘液がたまり、気道の粘膜に刺激と損傷を与える。CFの治療には、気道確保とも呼ばれる胸部理学療法があり、様々な機器や手技を用いてこの粘液を取り除く。運動にも同様の効果があることが示唆されている。運動をすると、人はさまざまな量と深さの呼吸をすることになる。その結果、気道内の圧力変化と力の変化が生じ、分泌物が肺の外に移動する。運動がCF患者の肺機能に与える影響を他の手法と比較し、運動がCF患者の代替手段として適切かどうかを検討した。CF患者の治療負担を軽減する可能性のあるレビューの論点に答えたいと考えた。 検索期間 エビデンスは2022年2月15日までのものである。 研究の特性 運動または他の気道確保技術の治療セッションを少なくとも2回受けた研究を文献検索し、このレビューでは86人のCFを含む4件の研究について報告する。研究対象者は7歳から41歳までで、病気の重症度もさまざまであった。3件の研究では、臨床的に健康な人を対象とし、1件の研究では、胸部感染症で入院した人を対象とした。研究期間は4日から6か月で、運動(単独または他...

頸動脈内膜剥離術のための日常的または選択的な頸動脈シャント術(および選択的シャント術における異なるモニタリング法)

2 years 11 months ago
頸動脈内膜剥離術のための日常的または選択的な頸動脈シャント術(および選択的シャント術における異なるモニタリング法) 論点 全身麻酔下頸動脈内膜剥離術を受ける患者を対象に、シャント術が脳卒中、死亡、その他の合併症にどのように影響するか、また、選択的シャント術のモニタリング法の違いがこれらの結果にどのように影響するかを検討した。 背景 脳卒中の約20%は、頸動脈(脳に血液を供給する主動脈)の狭窄が原因である。頸動脈内膜剥離術は、この狭窄を取り除くことで脳卒中リスクを低減する手術である。しかし、脳卒中を引き起こす手術時リスクは2%~3%ある。一時的なバイパスとしてシリコンチューブ(シャント)を使用することで、術中に脳への血流が遮断される時間を短縮することができる。これにより、周術期の脳卒中リスクを低減できる可能性があるが、動脈壁の損傷を招き、その結果、脳卒中リスクが高まる可能性もある。シャント手術は、3つのカテゴリーに分類される。第一に、日常的シャント術では、外科医はすべての患者さんにシャントを挿入する。第二に、選択的シャント術では、術者はクランプ後に脳への血液供給が不十分な患者にのみシャントを使用する。この方針では、シャントが必要な人を予測するための超音波検査など、さまざまな脳血流モニタリング技術が用いられてきた。第三に、シャント術なしとは、外科医がシャントを全く使用しないことである...

Ivermectin for preventing and treating COVID-19

2 years 11 months ago

Is ivermectin effective for COVID‐19? Updated Cochrane review 'Ivermectin for preventing and treating COVID‐19'

Key messages

  • We found no evidence to support the use of ivermectin for treating COVID‐19 or preventing SARS‐CoV‐2 infection. The evidence base improved slightly in this update, but is still limited.
  • Evaluation of ivermectin is continuing in 31 ongoing trials, and we will update this review again when their results become available.  

What is ivermectin?
Ivermectin is a medicine used to treat parasites, such as intestinal parasites in animals, and scabies in humans. It is inexpensive and is widely used in regions of the world where parasitic infestations are common. It has few unwanted effects.  

Medical regulators have not approved ivermectin for COVID‐19.

What did we want to find out?
We wanted to update our knowledge of whether ivermectin reduces death, illness, and length of infection in people with COVID‐19, or is useful in prevention of the infection. We included trials comparing the medicine to placebo (dummy treatment), usual care, or treatments for COVID‐19 that are known to work to some extent, such as dexamethasone. We excluded trials comparing ivermectin to other medicines that do not work, like hydroxychloroquine, or whose effectiveness against COVID‐19 is uncertain.

We evaluated the effects of ivermectin in infected people on:

  • people dying;
  • whether people's COVID‐19 got better or worse;
  • quality of life;
  • serious and non‐serious unwanted effects;
  • viral clearance.

For prevention, we sought the effect on preventing SARS‐CoV‐2 infection and COVID‐19 disease.

What did we do?
We searched for randomized controlled trials that investigated ivermectin to prevent or treat COVID‐19. People treated in hospital or as outpatients had to have laboratory‐confirmed COVID‐19.

In this update, we also investigated the trustworthiness of the trials and only included them if they fulfilled clear ethical and scientific criteria.

We compared and summarized the results of the trials and rated our confidence in the evidence, based on common criteria such as trial methods and sizes.



What did we find?
We excluded seven of the 14 trials included in the previous review as these trials did not fulfil the expected ethical and scientific criteria. Together with four new trials, we included 11 trials with 3409 participants that investigated ivermectin combined with any usual care compared to the same usual care or placebo.

For treatment, there were five trials of people in hospital with moderate COVID‐19 and six trials of outpatients with mild COVID‐19. The trials used different doses of ivermectin and different durations of treatment.  

No trial investigated ivermectin to prevent SARS‐CoV‐2 infection.

We also found 31 ongoing trials, and an additional 28 trials still requiring clarification from the authors or not yet published.

Main results  

Treating people in hospital with COVID‐19

We do not know whether ivermectin compared with placebo or usual care 28 days after treatment:

  • leads to more or fewer deaths (3 trials, 230 people);
  • worsens or improves patients' condition, assessed by need for ventilation or death (2 trials, 118 people);
  • increases or reduces serious unwanted events (2 trials, 197 people).

Ivermectin compared with placebo or usual care 28 days after treatment, may make little or no difference to:

  • improving patients' condition, assessed by discharge from hospital (1 trial, 73 people);
  • non‐serious unwanted events (3 trials, 228 participants). 

Seven days after treatment, ivermectin may make little or no difference to reduction of negative COVID‐19 tests (3 trials, 231 participants) compared with placebo or usual care.

Treating outpatients with COVID‐19
Ivermectin compared with placebo or usual care 28 days after treatment, probably makes little or no difference to people dying (6 trials, 2860 people).

Ivermectin compared with placebo or usual care 28 days after treatment, makes little or no difference to quality of life (1 trial, 1358 people).

Ivermectin compared with placebo or usual care 28 days after treatment, may make little or no difference to:

  • worsening patients' condition, assessed by admission to hospital or death (2 trials, 590 people);
  • serious unwanted events (5 trials, 1502 people);
  • non‐serious unwanted events (5 trials, 1502 participants);
  • improving people's COVID‐19 symptoms in the 14 days after treatment (2 trials, 478 people);
  • number of people with negative COVID‐19 tests 7 days after treatment (2 trials, 331 people).

Review authors, Dr Maria Popp and Dr Stephanie Weibel said:

“Overall, the outlook for ivermectin’s use to treat or prevent SARS-CoV-2 is poor. While laboratory results showed some promise, real-life outcomes suggest no or very little impact on mortality rates, illness, and length of infection.”

What are the limitations of the evidence?
Our confidence in the evidence, especially for outpatients, improved since the last review version, because we could look at more participants included in high‐quality trials. Although we are quite certain regarding our results on risk of people dying and quality of life, the confidence in the evidence is still low for many other outpatient and inpatient outcomes because there were only few events measured. The methods differed between trials, and they did not report everything we were interested in, such as relevant outcomes.

How up to date is this evidence?
The systematic literature search is up to date to 16 December 2021. Additionally, we included trials with > 1000 participants up to April 2022.

 

Wednesday, June 22, 2022
Katie Abbotts

肩を骨折した成人に最も適した治療法は何か

2 years 11 months ago
肩を骨折した成人に最も適した治療法は何か 要点 ‐腕吊りを1週間使用した後、早い時期に腕を動かすと、3 週間またはそれ以上腕吊りで腕を固定する場合に比べて、長期的な肩の機能や肩の問題の発生に違いがあるかは、エビデンス(科学的根拠)が十分でないため、判断できない。 ‐患者の報告によると、転位を伴う(折れた骨片がずれてしまった)大半の種類の骨折では、手術をしても、手術以外の治療より肩の機能がよくなるとは言えない。他方、合併症ゆえに再手術が必要になるリスクが高まる可能性がある。 ‐手術を行う場合も、どの方法が一番よいか判断するには、エビデンスが十分ではない。 上腕骨近位端骨折とはなにか 上腕骨近位端とは二の腕の骨の上端である。上腕骨近位端骨折は、高齢者によく見られる大きなけがである。これは一般に肩の骨折と呼ばれる。患者が再び腕を使えるようになるまでに数か月かかることがある。よくある長期的な問題には、可動域の制限や痛みがある。 こうした骨折には通常どのような治療が行われるか 治療には以下のものがある。 ‐手術によらない治療:けがした腕を1週間またはそれ以上の期間にわたって腕吊りで支える。 ‐手術:折れた骨片がずれてしまった「転位を伴う骨折」について行われる。手術では、骨折片を元の位置に戻し、金属プレートとねじで留めたり、骨髄内に釘を挿入して固定したりする。あるいは、高齢者の場合、肩の球関...

土壌伝播蠕虫感染症予防のための水・衛生・保健衛生改善への介入

2 years 11 months ago
土壌伝播蠕虫感染症予防のための水・衛生・保健衛生改善への介入 レビューの目的 このレビューは、土壌伝播蠕虫感染症の感染予防に関する水・衛生・保健衛生活動の効果を評価したランダム化比較試験(RCT)(参加者を2つ以上の治療群のいずれかに無作為に割り付ける試験)と非ランダム化試験(非RCT)を要約したものである。 土壌伝播蠕虫(STHs)は、腸内寄生虫の一種で、土壌や水源を汚染した人間の糞便中に排泄された感染性卵の摂取や幼虫の経皮(皮膚からの)侵入により人間に感染する。駆虫を行ったとしても、再感染が急速に進むため、補完的な対策なくしては、感染の阻止は難しい。再感染を抑え、病気を減らすためには、安全で十分な水、基本的衛生設備、衛生(WASH)へのアクセスと利用などの環境改善が不可欠と考えられている。 主な結果 このエビデンスは、研究中のWASHの介入がSTH感染をわずかに減少させる可能性があることを示唆している。これらの結果の多くは、治療群と対照群の両方で大量薬剤投与を行った研究であり、大量薬剤投与の適用以上のSTH感染に対するWASHの影響を示している。 本レビューで検討された内容 WASHとSTH感染症を評価するこれまでのレビューは、非実験的な研究に大きく依存している。STH感染を減らすためのWASHプログラムの役割を評価する厳密で実験的なエビデンスを調査した。 レビューの主な結果...

ピロナリジン-アーテスネートによる合併症のない熱帯熱マラリア原虫によるマラリアの治療法

2 years 11 months ago
ピロナリジン-アーテスネートによる合併症のない熱帯熱マラリア原虫によるマラリアの治療法 レビューの目的 このコクランレビューの目的は、抗マラリア薬であるピロナリジン・アーテスネートが、重要なタイプのマラリア(熱帯性マラリア原虫)の合併症のない症例に対して有効かつ安全であるかどうかを調べることであった。この疑問に答えるため、関連するすべての研究を収集・分析したところ、10件の研究が見つかった。 主な結果 ピロナリジン-アーテスネートは、合併症のない熱帯熱マラリア原虫によるマラリアの治療に有効である。ピロナリジン-アーテスネートは一般的に安全であるが、投与された人の中には血液検査で肝障害が示唆される人がいる。これは長続きしないし、病気にもならないようだ。 本レビューで検討された内容 世界保健機関(WHO)は、アルテミシニン系複合療法(ACT)と呼ばれる薬剤の組み合わせでマラリアを治療することを推奨している。ピロナリジン・アーテスネートは新規のACTである。現在使用されているACTに耐性を持つようになったマラリアを治療するため、また、マラリアが治療に対してより耐性を持つようになるのを防ぐために、新しいACTが必要とされている。 熱帯熱マラリア原虫によるマラリアに対する有効性を評価するためにピロナリジン・アーテスネートと他のACTを比較し,安全性を評価するためにピロナリジン・アーテスネー...

Cochrane Rapid Reviews Methods Group seeks graduate research assistant - Flexible location

2 years 11 months ago

Specifications: 20 hours/week until 31 December, 2022
Salary: £1,500 per month
Location: Flexible Location, Remote Work
Application Closing Date:  3 July, 2022

The Cochrane Rapid Reviews Methods Group is currently looking for a Graduate Research Assistant with experience in rapid or systematic reviews for 20 hours/week (temporary position until December 31, 2022).

Required qualifications:

  • Graduate or PhD student in the field of health care (medicine, public health, biology, psychology, nursing science etc.)
  • Good understanding of rapid reviews
  • Experience in conducting systematic reviews
  • Excellent writing skills in English (C1)

Tasks: 

  • Support the Cochrane Rapid Reviews Methods Group (CRRMG) in providing rapid review guidance for the Cochrane Handbook, the Rapid Review Methods Guidance, and journal publications
  • Support the CRRMG with scheduling and preparing workshops
  • Communicate and collaborate with various other groups at Cochrane (e.g., editorial team)

Benefits:

  • Flexible working hours
  • 100% remote working possible

The successful candidate will be hired by Cochrane Austria at the University for Continuing Education Krems, Austria. The salary will be 1500 EUR per month. All applications must be submitted by Sunday, July 3, 2022 per email at office@cochrane.at

Please include: 

  • Curriculum vitae
  • Cover letter
  • Certificates

If you have any questions, please contact Sandra Hummel (office@cochrane.at).

We look forward to hearing from you! 

Monday, June 20, 2022 Category: Jobs
Muriah Umoquit

がん患者の貧血の予防と治療に最善な薬剤の組み合わせの検討

2 years 11 months ago
がん患者の貧血の予防と治療に最善な薬剤の組み合わせの検討 要点 • 骨髄を刺激して赤血球を産生する薬剤(ESA)を鉄剤と一緒に投与すると、輸血回数が減少することはほぼ確実であるが、死亡率の上昇をもたらし、血栓(血の塊)など望ましくない副作用が増えるおそれもある。 • 各研究に欠測データがあったため、さまざまな治療選択肢を相互に比較して順位をつけることができなかった。 • 各薬剤を相互に直接比較する研究がさらに必要である。 貧血とは何か、なぜがんがあると貧血になるのか 赤血球が少なくなりすぎると貧血になる。赤血球には、ヘモグロビンというタンパク質が含まれている。ヘモグロビンの構成成分である鉄分子が、酸素と結合して体中に酸素を運ぶ。体内の臓器や組織が酸素不足になると疲れやすくなって元気がなくなり、感染症のリスクが高くなる恐れもある。がんがある人は特に貧血になりやすい。これは、がんが炎症を起こし、赤血球の産生を妨げるためと思われる。または、化学療法などの治療によって、骨髄での赤血球の産生が鈍くなるせいかもしれない。 貧血の人には輸血が必要になることもある。しかし、骨髄での赤血球の産生を促進する(赤血球造血刺激因子製剤またはESAと呼ばれる)薬剤や鉄剤による治療によって輸血の必要性が減るのではないかと思われる。 知りたかったこと がん患者の貧血に最も効果的な治療法と、その治療法が好ましく...

How to talk about vaccines when you’re not an expert: a Lifeology and Cochrane collaboration

2 years 11 months ago

In this free course, learn how you can talk about vaccines with anyone!

Just because you’re a researcher, clinician, or  scientist doesn't mean that you should know everything about viruses and vaccines…but you may be asked to talk about them! It's important to remember that these conversations aren’t just about facts and information. They can be an opportunity to build trust and advocate for science! ‘How to talk about vaccines when you’re not an expert’ is a free Lifeology course that walks you through practical tips that you can apply next time you’re asked about the topic.

Lifeology’s tagline is ‘The place where science and art converge’. They offer a platform that brings together scientists, artists, and storytellers to help people better understand and engage with science, health information, and research. One of the main ways they meet their objectives is through beautifully illustrated, evidence-informed, bite-sized ‘flashcard’ courses about science and health-related topics aimed at the general public and students. There have been other collaborations with Cochrane on courses, including ‘What is an infodemic and how can we prevent it?’ and 'How to communication scientific uncertainty.'

 

“This course was inspired by real events – and one many can relate to!” explains author Muriah Umoquit, Cochrane’s Communications and Engagement Officer. “I baked 7 dozen cookies and found myself at a cookie exchange…where everyone was against the COVID-19 vaccine. As a professional health communicator, I felt like I should educate them with the latest studies and dazzle them into being pro-science over our appetizers! But instead, I froze. And when the subject changed, I left. It was a missed opportunity and one that many researchers and scientists find themselves in. This course gives practical advice to draw from, so we can all be more confident in our conversations about vaccines or other health or science conversations.”

The course has  22 cards that share the story of a systematic reviewer asking their colleague for advice when talking about vaccines. It features the art of Abbey Morris. “When creating the illustrations, I made a conscious effort to use inclusive imagery and avoided adding any text that would hinder future language translations,” Abby explains. “I also hope the Cochrane Community will enjoy some  hidden ‘Easter Eggs’ in this course just for them!”

Ruobing Li researches vaccine hesitancy at the Alan Alda Centre for Communicating Science and also collaborated on this project with us by  reviewing the content. “Sharing science is not just about sharing facts and information. This course is short, practical in its advice, and really accessible. Trust in science isn’t built in one conversation; I hope this course will encourage and give confidence to all scientists and researchers to have many conversations!”


Having a course that would be assessable in multiple languages was also built into its design. Juan Franco, Cochrane Board Member, family physician, researcher, and Editor-in-Chief of Evidence-Based Medicine was another reviewer of this course. "Muriah and her colleagues designed this course knowing that we wanted to make it assessable to a global audience through our amazing Cochrane Translation Teams" Juan explains. "For this reason, we provided feedback to be sure to avoid words in the illustrations, cultural-specific analogies or phrases, and complex words. The end result makes for a great course in any language!"

View the Lifeology course ‘How to talk about vaccines when you’re not an expert' in:

Learn more about Lifeology: 

Wednesday, December 7, 2022
Muriah Umoquit

人工のCOVID-19特異的モノクローナル抗体は、成人におけるCOVID-19の予防に有効か?

2 years 11 months ago
人工のCOVID-19特異的モノクローナル抗体は、成人におけるCOVID-19の予防に有効か? 要点 COVID-19の曝露前の予防: - チキサゲビマブ/シルガビマブは、COVID-19の感染者数およびCOVID-19症状の発現をおそらく減少させ、入院者数を減少させる可能性がある; - カシリビマブ/イムデビマブは、COVID-19の感染者数およびCOVID-19症状の発現を減少させる可能性があり、好ましくない影響(重症度を問わず)がわずかに増加する可能性がある; COVID-19の曝露後の予防: - バムラニビマブはCOVID-19の感染者数を減少させると思われる; - カシリビマブ/イムデビマブは、COVID-19の感染者数およびCOVID-19症状の発現を抑制し、好ましくない影響(重症度を問わない)の発現を抑制する。 モノクローナル抗体とは何か? 病気から身を守るために、体は抗体を作る。しかし、病気より回復した人から採取した細胞から人工的に作ることもある。 特定の1つのタンパク質のみを標的とする抗体が「モノクローナル抗体」である。この場合、SARS-CoV-2ウイルス(COVID-19の原因)のタンパク質である。それらはウイルスに付着して、ヒトの細胞内への侵入や複製を阻止し、感染を予防し撃退する。それらは予防接種に反応しない人、反応が悪い人に関係する。 何を知りたかったの...

Author Q&A: Does treatment for gum disease help people with diabetes control blood sugar levels?

2 years 11 months ago

We spoke to Cochrane Oral Health Author Terry Simpson about the updated review Treatment of periodontitis for glycaemic control in people with diabetes mellitus. He explains the results of this review and what it means for the research community as well as medical, nursing, and dental professionals - with thanks also to Josh Twigg, Ambrina Qureshi, Sarah Wild, Ian Needleman and Laura MacDonald.

Terry, can you tell us about this updated Cochrane Review?
Our review of studies evaluating the impact of treatment of periodontitis (gum disease) on glycaemic control in people with diabetes was originally published in 2010 (based on a protocol published in 2004) and first updated in 2015. For the 2022 update, we divided the review in two due to the sheer volume of studies on this topic and to account for the clear divide that has emerged in the research, focusing on two different key questions. This update answers the question: how does treatment of periodontitis compare to usual care or no treatment for improving glycaemic control in people with diabetes; the second part of the update will compare different approaches to treatment of periodontitis against one another, to assess if there is a gold standard for treatment.

This first part of our update found that glycaemic (blood sugar) control in people with diabetes can be improved with treatment of periodontitis. The improvement in diabetic control from treating any periodontitis appears to be approximately equivalent to the threshold for determining effectiveness of an additional diabetes drug - but without the side effects.



What does it mean for the research community?
For the first time since this review began, we have shown that we do not need to conduct further randomised controlled trials that compare periodontal treatment against no treatment or usual care in people who have both diabetes and periodontitis. Within the population of people with diabetes, there is the potential for individuals to improve glycaemic control through treating their periodontitis and therefore we recommend that research should not withhold periodontal treatment from such people for the purpose of a research study that is highly unlikely to add new information to the evidence base. Trials comparing different approaches to periodontal treatment may still be useful, while qualitative studies and process evaluations will be helpful to establish how best to optimise the provision of effective periodontal treatment in primary care settings and to support patients to improve their periodontal health and oral hygiene practices.

Given the evidence is clear, what needs to change?
As treatment of periodontitis in people who also have diabetes can have a beneficial effect on metabolic control (glycaemic levels), it is important that there is better communication between dental and medical professionals managing patients with diabetes and periodontitis as this will facilitate appropriate treatment to minimise risk of complications of diabetes. Unfortunately, care pathways between diabetes and oral health do not exist for most patients. Therefore, healthcare policy and guidance are needed to establish such funded pathways.

For dental professionals, greater awareness is required regarding effective monitoring and treatment of diabetic patients with periodontitis. Professional development for all relevant healthcare staff (including diabetologists, other medical and nursing teams dealing with diabetic patients and the dental professionals) must be delivered to transfer knowledge, address barriers and support implementation. Partnering with organisations that provide information and support for people with diabetes and oral health would be helpful.

Governments may wish to review how socially funded health schemes are addressing the need for periodontal care, particularly among people with diabetes, where the potential for improvement in health and quality of life may be profound. The role of periodontal specialists in providing training and advice on referral for further management is critical in ensuring the dental workforce is equipped to manage this group of patients to the best standard.  

Groups formulating guidelines on diabetes or periodontitis should incorporate the findings of our review so that appropriate educational resources are available for professionals and patients. In the UK, we are aware that NICE have already undertaken this responsibility.



How can clinicians working in this field change what they do?
Medical and nursing professionals should ask all patients diagnosed with diabetes whether they have had a dental visit to get their gums checked and to emphasise the importance of gum health in diabetes management. They can signpost or refer their patients to dental professionals in the case of any unusual presentation or poor oral health identified during general screening on follow-up visits. Similarly, dental professionals (dentists and hygienists/therapists) can advise all patients with diabetes of their increased risk of gum disease and the benefits of good gum health for their overall health and wellbeing. Regular screening of gum health should continue to be provided to all patients, with detailed assessment for those identified at risk of periodontitis. Most patients will continue to be suitable for treatment under the care of a general dentist. However, for people with more severe gum disease and where gum disease is not responding to treatment, referral to a specialist (periodontist) should be considered where available.

Dental and medical professionals can familiarise themselves with the evidence about the links between periodontitis and diabetes. Both professions can assist in the process of educating patients about this relationship. Dentists can play a role in screening for diabetes, considering the possibility of undiagnosed diabetes in patients with risk factors (such as increasing age, higher BMI, non-white ethnicity, family history of diabetes) and the presence of periodontitis, particularly when the condition is severe. They should be able to inform patients of local options for testing for diabetes.

Where can clinicians find out more?

Thursday, June 16, 2022
Lydia Parsonson

なぜ認知症診断の向上が重要なのか?

2 years 11 months ago
なぜ認知症診断の向上が重要なのか? 認知症とは、日常生活における記憶、物事への取り組み、または機能などに進行性の問題が生じる、脳の疾患群のことを指す。医師は認知症の診断のために様々な検査を行う。認知症を疑わせる症状で医療機関を受診してから、認知症と診断されるまでに長い時間がかかることがよく報告されている。 認知機能障害とは、認知症の方だけでなく、年齢的に脳の機能が低下しているが、認知症ではない方も含む、より広い意味の用語である。認知症でない認知機能障害者の中には、軽度認知障害(MCI)と呼ばれる状態にある人もいる。MCIの人の中には、時間が経つにつれて認知症を発症する人もいる(全員ではない)。 レビューの目的 このレビューは、プライマリケアにおける認知症、および認知機能障害の診断における総合診療医(GP)の臨床判断の診断精度を検討した。 レビューでは何を調べたのか? 診断精度に関する完全なデータを有する10件を含む11件の研究からの抽出データを対象とした。合計2,790人を対象とした8件の研究を統計的要約に含め、そのうち826人(30%)が認知症であった。診断する状態として認知機能障害を調査した4件の研究を対象とし、合計1,497人のうち594人が認知機能障害(40%)であった。 レビューの主な結果は何か? レビューの結果、理論的には、総合診療医が認知症の診療において臨床判断を行...

World EBHC Day campaign addresses global health challenges through partnerships for purpose

2 years 11 months ago

JBI, Cochrane, Campbell, GIN, the Institute for Evidence-Based Healthcare, the Centre for Evidence-based Health Care, and NICE recently launched the World Evidence-Based Healthcare (EBHC) Day 2022 campaign, ‘Partnerships for Purpose’. 

World EBHC Day is held on 20 October each year. It is a global initiative that raises awareness of the need for better evidence to inform healthcare policy, practice and decision making in order to improve health outcomes globally. It is an opportunity to participate in debate about global trends and challenges, but also to celebrate the impact of individuals and organisations worldwide, recognising the work of dedicated researchers, policymakers and health professionals in improving health outcomes.

The 2022 campaign aims to examine partnerships and practical considerations around establishing different types of partnerships, accelerating innovation, ensuring equity and integrity, overcoming challenges and biases, lessons learned and achieving impact for improved health outcomes globally.

 

There is a growing concern, which was heightened during the pandemic, about making partnerships and collaboration equitable for — and beneficial to — all partners. Although willingness to collaborate has increased, vested interests, bureaucracy and inability to change remain limiting factors. Around the globe, organisations have set up networks, task forces and working groups to coordinate efforts and overcome some of these challenges.

Cochrane’s Editor in Chief, Dr Karla Soares-Weiser says, 

"Partnerships are at the heart of evidence-informed healthcare, and I am very proud of the work Cochrane does with our partners. As a global evidence community, we know that we need to work together to coordinate efforts and make the best use of limited resources. Working together is also an opportunity to listen to and learn from other perspectives, ultimately to benefit the health of all worldwide. I look forward to the discussions that this year’s World EBHC Day campaign on partnerships for purpose will generate."

World EHB Day Events

  • Talking the walk: equity in global health partnerships 
    • 19 October 2022
    • Free webinar
    • In this 90-minute moderated discussion we will hear from key global experts who challenged the status quo of what ‘equity’ means in global health partnerships, including open and engaging conversations with participants.  Includes Tamara Kredo, Deputy Director and Chief Specialist Scientist at Cochrane South Africa. 
  • Making health decisions: what’s best for you?
    • 20 Oct 2022
    • Free webinar
    • Hosted by Cochrane UK, this webinar will equip you with some questions and considerations that you can reflect on and discuss with a healthcare professional – to help you make the best health decision for you.
  • Cochrane and Partnerships
    • 20 Oct 2022
    • Free webinar
    • Hosted by Cochrane US Network, this webinar will focus on why partnerships are important across the spectrum - from your own life to healthcare policy and practice. Come hear from three Cochrane Board members and three Cochrane US mentees.

Cochrane World EBHC Day Blogs

Cochrane World EBHC Day Vlogs


 

Wednesday, October 19, 2022
Muriah Umoquit

入院中の子どもや若者の睡眠を薬を使わずに促進する方法(非薬物療法)

2 years 11 months ago
入院中の子どもや若者の睡眠を薬を使わずに促進する方法(非薬物療法) 主な結果 入院中の子どもや若者に対して、薬物以外の睡眠促進方法がどの程度有効なのかは不明である。 入院中の子どもや若者を対象に、薬物以外の睡眠促進について調査し、効果のある方法を特定するために、確立された信頼性の高い研究方法を用いた研究が必要である。 入院中の子どもにとって、なぜ睡眠が大切なのか? 睡眠は、子どもの健全な発育に重要な役割を果たし、子どもの健康維持に役立つ。睡眠パターンは、子どもの脳の発達に伴い、子ども時代を通じて変化する。子どもが病気になり入院すると、騒音や光、医療行為、看護師による監視、ストレス、痛みなどで、睡眠の質が低下したり、睡眠が妨げられたりすることがある。 入院している子どもの睡眠を改善しようと薬を使うこともあるが、特に効果がなく、睡眠の質を悪化させることもあるという研究結果が出ている。薬以外の方法で睡眠を促進することも可能である。その方法としては、病院の環境を変える、音楽をかける、マッサージをするなどが考えられる。 知りたかったこと 入院している子どもたちに対して、睡眠を改善しようとする薬以外の方法が、通常のケアや他の方法よりもうまくいくかどうかを調べたいと考えた。 これらの異なる方法が以下の項目に対してどの程度有効なのかを調べたいと考えた。 - 子どもたちの睡眠の質と量; - 子ども...

Cochrane seeks Statistical Editor - Flexible location

2 years 11 months ago

Specifications: Part time 22.5 hours (Permanent/Consultancy role considered)
Salary: £45,000 per annum full time equivalent
Location: Flexible
Application Closing Date:  27 June 2022

The Evidence Production and Methods Directorate in Cochrane is made up of three departments that are responsible for the efficient and timely publication of high-quality systematic reviews in the Cochrane Library. One of the three departments is the Methods and Evidence Synthesis Development team.

The Methods Support Unit (MSU) sits in the Methods and Evidence Synthesis Development team. The MSU provides hands on statistical and methods support to people preparing Cochrane systematic reviews. As Statistical Editor, you will provide advanced methods support and advice as requested by the Methods Support Unit Manager, from members of the Cochrane community directly or via  the Community Support Team as needed. The post holder will also provide independent methods review of high-profile reviews, including those intended for press release. In addition to this you will support the implementation of established and more complex methods in Cochrane reviews and work on monitoring the quality of statistical methods and analysis in Cochrane reviews to inform priorities for training and guidance. The role will require a formal qualification in epidemiology or biomedical statistics, and a good understanding of methods used in meta-analysis.

Cochrane is a global, independent network of health practitioners, researchers, patient advocates and others, responding to the challenge of making vast amounts of research evidence useful for informing decisions about health. We do this by synthesizing research findings to produce the best available evidence on what can work, what might harm and where more research is needed. Our work is recognised as the international gold standard for high quality, trusted information. An understanding of Cochrane’s work and health research more generally is an advantage, but not essential.

The majority of Cochrane Central Executive staff are located in London, UK, however flexible location or a part-time appointment are possible for the right candidate.

How to apply

  • For further information on the role and how to apply, please click here
  • The deadline to receive your application is by 27 June 2022. 
  • The supporting statement should indicate why you are applying for the post, and how far you meet the requirements, using specific examples.
  • Note that we will assess applications as they are received, and therefore may fill the post before the deadline.
  • Interviews to be held on: w/c 11 July 2022
  • Read our Recruitment Privacy Statement 
Tuesday, June 14, 2022 Category: Jobs
Lydia Parsonson

Cochrane seeks Methods Support Unit Manager - UK

2 years 11 months ago

Specifications: Permanent
Salary: £52,000 per annum
Location: UK
Application Closing Date:  27 June 2022

The Evidence Production and Methods Directorate in Cochrane is made up of three departments that are responsible for the efficient and timely publication of high-quality systematic reviews in the Cochrane Library. One of the three departments is the Methods and Evidence Synthesis Development team.

The Methods Support Unit (MSU) sits in the Methods and Evidence Synthesis Development team. The MSU provides hands on statistical and methods support to people preparing Cochrane systematic reviews. As lead for the Methods Support Unit, you will be responsible for ensuring that people preparing reviews for publication in the Cochrane Library have access to current advice about the implementation of systematic review methods, including searching, statistical analysis, and bias assessment. The team comprises a Systematic Review Methodology Editor, a Statistical Editor and an Information Specialist. Additional budget will be made available to fund additional methods expertise as may be required.

The Methods Support Unit Manager will be responsible for ensuring that methodological and statistical queries from the Evidence Synthesis Development Editors, Editorial Service or Cochrane Support Team are addressed. The role will require a formal qualification related to systematic review methods.

How to apply

  • For further information on the role and how to apply, please click here
  • The deadline to receive your application is by 27 June 2022. 
  • The supporting statement should indicate why you are applying for the post, and how far you meet the requirements, using specific examples.
  • Note that we will assess applications as they are received, and therefore may fill the post before the deadline.
  • Read our Recruitment Privacy Statement 
Tuesday, June 14, 2022 Category: Jobs
Lydia Parsonson

Cochrane International Mobility - Filip Wikström

2 years 11 months ago

Cochrane is made up of 11,000 members and over 67,000 supporters come from more than 130 countries, worldwide. Our volunteers and contributors are researchers, health professionals, patients, carers, people passionate about improving health outcomes for everyone, everywhere.

Getting involved in Cochrane’s work means becoming part of a global community. The Cochrane International Mobility programme connects successful applicants with a placement in a host Cochrane Group, learning more about the production, use, and knowledge translation of Cochrane reviews. The programme offers opportunities for learning and training not only for participants but also for host staff.

In this series, we profile those that have participated in the Cochrane International Mobility Program and learn more about their experiences.

Name: Filip Wikström
Location:
Lund, Cochrane Sweden
CIM location:
Barcelona, Cochrane Iberoamerica


How did you first learn about Cochrane?
The Cochrane Learning Modules are integrated into the Medicine Programme in Lund University, so I was gradually exposed to the Cochrane Methodology over several semesters. I think reading and assessing past research is an invaluable skill to have, so I was very glad to get the opportunity to do my Master’s Thesis with Cochrane.

What was your experience with Cochrane International Mobility?
My experience with the international mobility program was fantastic. The researchers at Cochrane Iberoamerica were very welcoming and I look back very fondly to the weeks I spent there. I learned a lot about systematic reviews but I also got to know amazing researchers and the projects they were working on.

What are you doing now in relation to your Cochrane International Mobility experience?
Currently I am contributing to a Cochrane Review on Tumor Necrosis Factor alpha inhibitors, under the supervision of Michele Compagno and Matteo Bruschettini (both based at Lund University). In the future I aspire to collaborate on more Cochrane projects.

Do you have any words of advice to anyone considering a Cochrane International Mobility experience?
Based on my own experience, I would advise anyone who likes systematic reviews to consider the program. It is a great opportunity to meet passionate researchers and work in an international environment. I got new perspectives on Cochrane methodology but also experiences that I think are important on a personal level.

 

 

Monday, June 20, 2022
Lydia Parsonson

Cochrane International Mobility - Agata Stróżyk

2 years 11 months ago

Cochrane is made up of 11,000 members and over 67,000 supporters come from more than 130 countries, worldwide. Our volunteers and contributors are researchers, health professionals, patients, carers, people passionate about improving health outcomes for everyone, everywhere.

Getting involved in Cochrane’s work means becoming part of a global community. The Cochrane International Mobility programme connects successful applicants with a placement in a host Cochrane Group, learning more about the production, use, and knowledge translation of Cochrane reviews. The prgramme offers opportunities for learning and training not only for participants but also for host staff.

In this series, we profile those that have participated in the Cochrane International Mobility Program and learn more about their experiences.

Name: Agata Stróżyk
Location:
Warsaw, Poland
CIM location:
Lund, Cochrane Sweden


How did you first learn about Cochrane?
I first got a chance to better know what systematic reviews are and what the role of Cochrane is when I was participating in the Evidence-Based Medicine faculty at my university. Systematic reviews are critical in summarizing clinical evidence and Cochrane is the most methodologically rigorous at doing it! In Poland, we call the Cochrane Handbook our Bible for systematic reviews.

What was your experience with your virtual Cochrane International Mobility?
To be a part of a Cochrane systematic review was definitely on my to-do list. I was looking for any opportunity to be involved in Cochrane for about two years. I was a supporter at Cochrane TaskExchange and Cochrane Crowd. Finally, I contacted Matteo at Cochrane Sweden, who involved me in a systematic review that was already ongoing. Thus, I didn’t have to go through all process, but from the beginning of my traineeship, I had to do specific tasks. Matteo and Giovanni Cagnotto (also based at Lund University) were my supervisors and are very friendly, kind, patient, and supportive at each step, but also very motivating and fast-working – that was a great experience!

What are you doing now in relation to your Cochrane International Mobility experience?
At the moment, we hope to complete our systematic review, “Tumor necrosis factor (TNF) inhibitors for the treatment of psoriatic arthritis”, in a couple of weeks. For sure, I will use what I’ve learned to do methodologically better systematic reviews in the future. Moreover, I will still look for other opportunities to be a part of the Cochrane community, and maybe one day to prepare a new Cochrane systematic review within my area of expertise.

Do you have any words of advice to anyone considering a Cochrane International Mobility experience?
If you are interested in systematic reviews, I think it is a highly desirable step to participate in any kind of traineeship supervised by Cochrane. For any medical practitioners and researchers who would like to better understand the critical appraisal of evidence and its translation into practice, I think it’s a great option too. My personal advice: do not give up, if you do not get any response for the first time! Be persistent in chasing your dreams

 

Monday, June 13, 2022
Lydia Parsonson

全身投与のヤヌスキナーゼ阻害剤は、COVID-19の患者にとって有効な治療法か?

2 years 11 months ago
全身投与のヤヌスキナーゼ阻害剤は、COVID-19の患者にとって有効な治療法か? 要点 入院患者におけるコロナウイルス感染症2019(COVID-19)に対して、全身投与のヤヌスキナーゼ(JAK)阻害剤は、死亡数が少なく、臨床的な悪化率が低いことから、有効な治療であると結論づける6件の研究を特定した。それらのエビデンスの確実性は中等度から高度であった。全身投与のJAK阻害剤の評価は13件の試験で進行中であり、さらに9件の試験では結果の公開待ちの状態である。それらの結果が利用可能になったときに、このレビューを更新して結論を変更する可能性がある。 JAK阻害剤とは何か? JAK阻害剤は、時に問題となる免疫システムの特定の部分の活動を阻害する薬である。これらは経口投与(全身投与)され、通常、免疫系が身体そのものを攻撃する自己免疫疾患を患っている人が服用する。JAK阻害剤は吸入での投与も可能であるが、今回は対象としていないため、レビュー全体を通して「全身投与のJAK阻害剤」と表記した。 JAK阻害剤はCOVID-19をどのように治療するのか? COVID-19では、時に免疫系が過剰に反応し、重篤な経過をたどることがある。JAK阻害剤は、免疫系の一部を阻害することで、臨床的な悪化を防ぐことができる。 何を知りたかったのか? COVID-19の患者に対して、通常のケアに加えて全身投与のJAK...